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rs587781730

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781730(-;-)
Make rs587781730(-;A)
Make rs587781730(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108307934
GeneATM
is asnp
is mentioned by
dbSNPrs587781730
ebirs587781730
HLIrs587781730
Exacrs587781730
Varsomers587781730
Maprs587781730
PheGenIrs587781730
hapmaprs587781730
1000 genomesrs587781730
hgdprs587781730
ensemblrs587781730
gopubmedrs587781730
geneviewrs587781730
scholarrs587781730
googlers587781730
pharmgkbrs587781730
gwascentralrs587781730
openSNPrs587781730
23andMers587781730
23andMe allrs587781730
SNP Nexus

SNPshotrs587781730
SNPdbers587781730
MSV3drs587781730
GWAS Ctlgrs587781730
Max Magnitude0
ClinVar
Risk rs587781730(A;A)
Alt rs587781730(A;A)
Reference rs587781730(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108178661dupA
CLNSRC
CLNACC RCV000129923.4, RCV000169006.1, RCV000212031.2,